- You J, Maksimovic K, Metri M, Chen K, Lee J, Schoeppe A, Santos J R, Youssef M, Salter M W & Park J#. Knockout of Dectin-1 does not modify disease onset or progression in a MATR3 S85C knock-in mouse model of ALS. Heliyon (2024). DOI: 10.1016/j.heliyon.2024.e37926. PMID: 39323783; PMCID: PMC11422021. (#: corresponding author)
Recent publications
- Santos J R & Park J#. MATR3’s Role beyond the Nuclear Matrix: From Gene Regulation to Its Implications in Amyotrophic Lateral Sclerosis and Other Diseases. Cells (2024). DOI: 3390/cells13110980. PMID: 38891112; PMCID: PMC11171696. (#: corresponding author)
- Khan M*, Chen X X L*, Dias M*, Santos J R*, Kour S, You J, van Bruggen R, Youssef M M M, Wan Y, Liu Z, Rosenfeld J A, Tan Q, Pandey U B, Yalamanchili H K#, Park J#. MATR3 pathogenic variants differentially impair its cryptic splicing repression function. FEBS Letters. (2024). DOI: 10.1002/1873-3468.14806 (*: co-first authors, #: co-corresponding authors)
- You J, Youssef M, Santos J R, Lee J & Park J. Microglia and astrocytes in amyotrophic lateral sclerosis: disease-associated states, contributing role in disease and therapeutic potential. MDPI Biology (2023) 12(10), 1307. DOI:10.3390/biology12101307
- Youssef M & Park J. LONRF2 is a gatekeeper against protein aggregation in aging neurons. Nature Aging (2023) DOI: 10.1038/s43587-023-00457-3. Epub ahead of print. PMID: 37474790.
- Maksimovic K, Youssef M, You J, Sung H.K., Park J. Evidence of Metabolic Dysfunction in Amyotrophic Lateral Sclerosis (ALS) Patients and Animal Models. Biomolecules (2023) 13(5):863. DOI: 10.3390/biom13050863. PMID: 37238732
- You J*, Maksimovic K*, Lee J, Khan M, Masuda R & Park J. Selective loss of MATR3 in spinal interneurons, corticospinal motor neurons and hippocampal neurons in a MATR3 S85C knock-in mouse model of amyotrophic lateral sclerosis. Biology (2022) 11(2), 298. DOI: 10.3390/biology11020298 (*: co-first authors)
- van Bruggen R*, Maksimovic K*, You J, Tran DD, Lee HJ, Khan M, Kao CS, Kim JR, Cho W, Chen XXL, Park J. MATR3 F115C knock-in mice do not exhibit motor defects or neuropathological features of ALS. Biochem Biophys Res Commun. 2021 Jun 25;568:48-54. PubMed PMID: 34182213. DOI: 1016/j.bbrc.2021.06.052 (*: co-first authors)
- Kao CS*, van Bruggen R*, Kim JR*, Chen XXL*, Chan C, Lee J, Cho WI, Zhao M, Arndt C, Maksimovic K, Khan M, Tan Q, Wilson MD, Park J. Selective neuronal degeneration in MATR3 S85C knock-in mouse model of early-stage ALS. Nat Commun. 2020 Oct 20;11(1):5304. PubMed Central PMCID: PMC7576598. DOI: 1038/s41467-020-18949-w (*: co-first authors)
- Zhao M*, Kao CS*, Arndt C, Tran DD, Cho WI, Maksimovic K, Chen XXL, Khan M, Zhu H, Qiao J, Peng K, Hong J, Xu J, Kim D, Kim JR, Lee J, van Bruggen R, Yoon WH, Park J. Knockdown of genes involved in axonal transport enhances the toxicity of human neuromuscular disease-linked MATR3 mutations in Drosophila. FEBS Lett. 2020 Sep;594(17):2800-2818. PubMed PMID: 32515490. DOI: 1002/1873-3468.13858 (*: co-first authors)
- Zhao M*, Kim JR*, van Bruggen R, Park J. RNA-Binding Proteins in Amyotrophic Lateral Sclerosis. Mol Cells. 2018 Sep 30;41(9):818-829. PubMed Central PMCID: PMC6182225. DOI: 14348/molcells.2018.0243 (*: co-first authors)
- Tan, Q.*, Yalamanchili, H.K.*, Park, J.*, De Maio, A., Lu, H., Wan, Y., White, J.J., Bondar, V.V., Sayegh, L.S., Liu, X., Gao, Y., Sillitoe, R.V., Orr, H.T., Liu, Z. & Zoghbi, H.Y. Extensive cryptic splicing upon loss of RBM17 and TDP43 in neurodegenerative models. Hum. Molec. Genet. (2016) 25(23):5083-93. PMID: 28007900. DOI: 10.1093/hmg/ddw337 (*: co-first authors) (cover)
- Park, J.*, Al-Ramahi, I.*, Tan, Q., Mollema, N., Diaz-Garcia, J. R., Gallego-Flores, T., Lu, H.-C., Lagalwar, S., Duvick, L., Kang, H., Lee, Y., Jafar-Nejad, P., Sayegh, L. S., Richman, R., Liu, X., Gao, Y., Shaw, C. A., Arthur, J. C., Orr, H. T., Westbrook, T. F., Botas, J. & Zoghbi, H. Y. RAS/MAPK/MSK1 pathway modulates Ataxin-1 protein levels and toxicity in SCA1. Nature (2013) 498(7454):325-31. PMID: 23719381. DOI: 10.1038/nature12204 (*: co-first authors)
- Park, J., Kim, Y. & Chung, J. Mitochondrial dysfunction and Parkinson’s disease genes: insights from Drosophila. Dis. Model Mech. (2009) 2(7-8):336-40. PMID: 19553694. DOI:10.1242/dmm.003178 (Review paper)
- Kim, Y.*, Park, J.*, Kim, S.*, Song, S., Kwon, S.K., Lee, S.H., Kitada, T., Kim, J.M. & Chung, J. PINK1 controls mitochondrial localization of Parkin through direct phosphorylation. Biochem. Biophys. Res. Commun. (2008) 377(3):975-80. PMID: 18957282. DOI: 10.1016/j.bbrc.2008.10.104 (*: co-first authors)
- Park, J.*, Lee, S. B.*, Lee, S., Kim, Y., Song, S., Kim, S., Bae, E., Kim, J., Shong, M., Kim, J. & Chung, J. Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkin. Nature (2006) 441(7097):1157-61. PMID: 16672980. DOI: 10.1038/nature04788 (*: co-first authors)